I5127
2′,3′-O-Isopropylideneuridine
≥99% (HPLC)
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关于此项目
经验公式（希尔记法）:
C12H16N2O6
化学文摘社编号:
分子量:
284.27
NACRES:
NA.51
PubChem Substance ID:
UNSPSC Code:
41106305
EC Number:
206-647-7
MDL number:
Assay:
≥99% (HPLC)
Biological source:
synthetic (organic)
Form:
powder
Solubility:
water: 50 mg/mL, clear to very slightly hazy, colorless to light yellow
Storage temp.:
−20°C
biological source
synthetic (organic)
Quality Level
assay
≥99% (HPLC)
form
powder
solubility
water: 50 mg/mL, clear to very slightly hazy, colorless to light yellow
storage temp.
−20°C
SMILES string
CC1(C)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O1)N3C=CC(=O)NC3=O
InChI
1S/C12H16N2O6/c1-12(2)19-8-6(5-15)18-10(9(8)20-12)14-4-3-7(16)13-11(14)17/h3-4,6,8-10,15H,5H2,1-2H3,(H,13,16,17)/t6-,8-,9-,10-/m1/s1
InChI key
GFDUSNQQMOENLR-PEBGCTIMSA-N
Application
2′,3′-O-Isopropylideneuridine is used in the chemical synthesis of N-benzoylated uridine derivatives and N3-substituted 2′,3′-O-isopropylideneuridines with central nervous system (CNS) depressant activity.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Tomomi Shimizu et al.
Chemical & pharmaceutical bulletin, 53(3), 313-318 (2005-03-04)
Seventy eight N(3)-substituted derivatives of uridine (1), thymidine (2), 2'-deoxyuridine (3), 6-azauridine (4), 2',3'-O-isopropylideneuridine (5), and arabinofuranosyluracil (6) were synthesized and their antinociceptive effects were evaluated. N(3)-(2',4'-Dimethoxyphenacyl)uridine (1l), N(3)-(2',4'-dimethoxyphenacyl)2'-deoxyuridine (3l), and N(3)-(2',5'-dimethoxyphenacyl)arabinofuranosyluracil (6m) possessed 93, 86, and 82% of the
C S Yao et al.
Chemical & pharmaceutical bulletin, 47(12), 1802-1804 (2000-04-05)
N3-Substituted derivatives of 2',3'-O-isopropylideneuridine (1) were synthesized and their pharmacological effects on the central nervous system (CNS) examined using mice. Methyl (2), ethyl (3), propyl (4), butyl (5), allyl (6), benzyl (7), o-, m-, p-xylyls (8, 9, 10), and alpha-phenylethyl
M L Scholes et al.
International journal of radiation biology, 61(4), 443-449 (1992-04-01)
The effect of pH on base release in the gamma-radiolysis of N2O-saturated solutions of a number of nucleosides (including uridine, 3-methyluridine, 2',3'-O-isopropylidene-uridine, and adenosine) has been investigated. For all these nucleotides, independent of the base or sugar moiety, base release
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| I5127-5G | 04061833857113 |
| I5127-25G | 04061833048436 |